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Structure of 207117-28-0
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral center at the alpha position, enabling stereoselective incorporation into peptide chains. The pendant hydroxyl group offers a handle for further functionalization, while the fluorenylmethoxycarbonyl moiety provides robust protection under standard coupling conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-2-methylpropanoic acid serves as a protected chiral building block for peptide synthesis, enabling efficient incorporation of hydroxylated amino acid motifs. The Fmoc group provides orthogonal protection with high stability under basic conditions and facilitates facile deprotection. The tertiary alcohol functionality offers a site for selective derivatization, while the methyl-substituted α-carbon enhances steric control in coupling reactions. Its bench-stable crystalline form simplifies handling and purification in standard synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: